Résumé
Abstract P III /P V redox cycling has recently emerged as a valuable strategy to minimized the chemical waste generated by phosphine‐mediated reaction, as well as enabling asymmetric transformation. In this article, we detail our contribution to this field by designing a series of diversely functionalized, electron‐rich bridgehead phosphine oxides with structural features that make them well‐suited as P III /P V redox organocatalysts. Their catalytic performance has been assessed in various model reactions, including Wittig or Staudinger reactions, along with the reduction of activated alkenes and allenes. For each of these scenarios, we performed a comparative analysis with existing catalysts in order to demonstrate the applicability and limitation of methanophosphocines.